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Gene Target
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Disease
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Evidence
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trials · metas · refs
Plus 6,743 TCM formulas connecting herbs together
18 Diseases matching "Homocystinuria"
Homocystinuria
Homocystinuria, Cbld Type, Variant 1
Homocystinuria, Pyridoxine-Responsive
Homocystinuria Due To Mthfr Deficiency
Homocystinuria, Pyridoxine-Nonresponsive
Homocystinuria Without Methylmalonic Aciduria
Homocystinuria Due To Deficiency of N(5,10)-Methyl
Homocystinuria-Megaloblastic Anemia Due To Defect
Mthfr Deficiency, Thermolabile Type
Methylcobalamin Deficiency, Cblg Type
Methylmalonic Acidemia With Homocystinuria
Methylmalonic Aciduria, Cbld Type, Variant 2
Hyperhomocysteinemia, Thrombotic, Cbs-Related
Cystathionine Beta-Synthase Deficiency Disease
Methylmalonic Aciduria And Homocystinuria, Cblj Ty
Methylmalonic Aciduria And Homocystinuria, Cbld Ty
Methylmalonic Aciduria And Homocystinuria, Cblc Ty
Methylmalonic Aciduria And Homocystinuria, Cblf Ty
🏥 Disease / Health Topic
Homocystinuria
2
Clinical Trials
0
Meta-Analyses
0
PubMed References
📋 Sample Trials
NCT02404337
Betaine METABOLISM OF PATIENTS With Homocystinuria
Completed · Phase 2
NCT01192828
Oxidative Stress Markers In Inherited Homocystinuria And The Impact Of Taurine
Completed · Phase 1|Phase 2
📊 Sample Meta-Analyses
None linked yet.
📚 Sample References
None linked yet.
🏥 All Disease / Health Topic data fields for Homocystinuria
🏥 Names
Disease Name
Homocystinuria
Alias Names
Homocystinuria; Cystathionine Beta-Synthase Deficiency Disease; High Urine Homocystine Levels
Topic Type
syndrome
🧬 Ontology Classifications
DisGeNET Type
disease
UMLS Type
Disease or Syndrome
MeSH Class
Nervous System Diseases; Skin and Connective Tissue Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
HPO Class
Abnormality of metabolism/homeostasis; Abnormality of the genitourinary system
DO Class
genetic disease; disease of metabolism
🔗 External References
🔍 Raw view — every non-empty column on this row (30 fields)
name
Homocystinuria
alias name
Homocystinuria; Cystathionine Beta-Synthase Deficiency Disease; High Urine Homocystine Levels
topic type
syndrome
disgenet disease type
disease
umls disease type
Disease or Syndrome
mesh disease class
Nervous System Diseases; Skin and Connective Tissue Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
hpo disease class
Abnormality of metabolism/homeostasis; Abnormality of the genitourinary system
do disease class
genetic disease; disease of metabolism
umls disease type id
T047
mesh disease class id
C16; C17; C18; C10
hpo disease class id
HP:0000119; HP:0001939
do disease class id
DOID:0014667; DOID:630
herb disease id
HBDIS001392
disgenet id
C0019880
mesh id
D006712
hpo id
HP:0002156
do id
9263
tcmsp disease id
378
📋 Clinical Trials
2 · subject of clinical studyNCT02404337 Betaine METABOLISM OF PATIENTS With Homocystinuria
→ Homocystinuria
NCT01192828 Oxidative Stress Markers In Inherited Homocystinuria And The Impact Of Taurine
→ Homocystinuria
How relationships are computed
- Clinical Trials / Meta-Analyses / References: direct foreign-key link via
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target_health_topics - Herb → Target → Disease (full chemical spine): ACTIVE — joins all three link tables